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WormBase Tree Display for Variation: WBVar00035831

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Name Class

WBVar00035831NamePublic_nameWBVar00035831
Other_namepas18763
cewivar00078808
W09B6.2c.1:c.522T>C
CE27222:p.Phe375=
CE51196:p.Phe301=
CE51162:p.Phe69=
W09B6.2b.1:c.903T>C
W09B6.2a.1:c.1125T>C
CE51176:p.Phe174=
W09B6.2d.1:c.207T>C
HGVSgCHROMOSOME_II:g.1131928T>C
Sequence_detailsSMapS_parentSequenceW09B6
Flanking_sequencesaagattcttgaacttttcggcataaaatctttgaaaatcgtgaatttcagtaaaaaattcaaatttccagttaatcgcgtgctgcaaacgcgccccacggccaatttatcagtggggcgcacttgtagcatgcgggcggcgggaaatttgaatttttgagttaaaaattcgatttttcaacgattttcgtcattttcaaggcattttttttgaattttttaaaatttccagagaccaagtggacaaacacgacgccggccgtaccgcccgtcgccttttcgatttttcgcatcgaattttcgcgacacgggctcctcgttctcgatgatctacggaaccgtccatatccttcaggaattcgtggcgggacccaaaaaagccgcttggctgctcacggagctcggcgagacgaatgcgcggtgcaaatcgcacatcgagtcgggctcacggatcggagcatcgcaactgtcgattcaggaggctcagaagcttaatcagcagattttggtaggtgtaaacgcgctctaatgagaaaatcgccgaattccggcgattttctcattggagcgcaattgctaaccttttttttttcagaaatgt
Mapping_targetW09B6
Type_of_mutationSubstitutionTC
SeqStatusSequenced
Variation_typeSNP
Predicted_SNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
Strain (64)
LaboratoryQX
AX
PersonWBPerson6900
WBPerson1730
AnalysisWGS_Pasadena_Quinlan
WGS_De_Bono
Million_mutation_project_reanalysis
WGS_Andersen
HistoryAcquires_mergeWBVar01293930
WBVar01359724
WBVar01435776
StatusLive
AffectsGeneWBGene00006387
TranscriptW09B6.2c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW09B6.2c.1:c.522T>C
HGVSpCE51176:p.Phe174=
cDNA_position522
CDS_position522
Protein_position174
Exon_number4/5
Codon_changettT/ttC
Amino_acid_changeF
W09B6.2b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW09B6.2b.1:c.903T>C
HGVSpCE51196:p.Phe301=
cDNA_position903
CDS_position903
Protein_position301
Exon_number6/7
Codon_changettT/ttC
Amino_acid_changeF
W09B6.2a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW09B6.2a.1:c.1125T>C
HGVSpCE27222:p.Phe375=
cDNA_position1141
CDS_position1125
Protein_position375
Exon_number8/10
Codon_changettT/ttC
Amino_acid_changeF
W09B6.2d.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScW09B6.2d.1:c.207T>C
HGVSpCE51162:p.Phe69=
cDNA_position207
CDS_position207
Protein_position69
Exon_number3/4
Codon_changettT/ttC
Amino_acid_changeF
ReferenceWBPaper00040707
WBPaper00037807
MethodWGS_Pasadena_Quinlan